Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Marian Hamshere"'
Autor:
Stéphane Jamain, Sven Cichon, Bruno Etain, Thomas W Mühleisen, Alexander Georgi, Nora Zidane, Lucie Chevallier, Jasmine Deshommes, Aude Nicolas, Annabelle Henrion, Franziska Degenhardt, Manuel Mattheisen, Lutz Priebe, Flavie Mathieu, Jean-Pierre Kahn, Chantal Henry, Anne Boland, Diana Zelenika, Ivo Gut, Simon Heath, Mark Lathrop, Wolfgang Maier, Margot Albus, Marcella Rietschel, Thomas G Schulze, Francis J McMahon, John R Kelsoe, Marian Hamshere, Nicholas Craddock, Markus M Nöthen, Frank Bellivier, Marion Leboyer
Publikováno v:
PLoS ONE, Vol 9, Iss 8, p e104326 (2014)
Bipolar disorder is one of the most common and devastating psychiatric disorders whose mechanisms remain largely unknown. Despite a strong genetic contribution demonstrated by twin and adoption studies, a polygenic background influences this multifac
Externí odkaz:
https://doaj.org/article/a0a21a9615324b178e8eea2ec3cbbf88
Autor:
Roy H, Perlis, Jie, Huang, Shaun, Purcell, Maurizio, Fava, A John, Rush, Patrick F, Sullivan, Steven P, Hamilton, Francis J, McMahon, Thomas G, Schulze, Thomas, Schulze, James B, Potash, Peter P, Zandi, Virginia L, Willour, Brenda W, Penninx, Dorret I, Boomsma, Nicole, Vogelzangs, Christel M, Middeldorp, Marcella, Rietschel, Markus, Nöthen, Sven, Cichon, Hugh, Gurling, Nick, Bass, Andrew, McQuillin, Marian, Hamshere, Nick, Craddock, Pamela, Sklar, Jordan W, Smoller
Publikováno v:
American Journal of Psychiatry, 167(12), 1499-1507. American Psychiatric Association
Perlis, R H, Huang, J, Purcell, S, Fava, M, Rush, A J, Sullivan, P F, Hamilton, S P, McMahon, S, Schulze, T, Potash, J B, Zandi, P P, Willour, V L, Penninx, B W J H, Boomsma, D I, Vogelzangs, N, Middeldorp, C M, Rietschel, M, Nöthen, M M, Cichon, S, Gurling, H, Bass, N, McQuillin, A, Hamshere, M L, Craddock, N, Sklar, P & Smoller, J W 2010, ' Genome-wide association study of suicide attempts in mood disorder patients ', American Journal of Psychiatry, vol. 167, no. 12, pp. 1499-1507 . https://doi.org/10.1176/appi.ajp.2010.10040541
Perlis, R H, Huang, J, Purcell, S, Fava, M, Rush, A J, Sullivan, P F, Hamilton, S P, McMahon, S, Schulze, T, Potash, J B, Zandi, P P, Willour, V L, Penninx, B W J H, Boomsma, D I, Vogelzangs, N, Middeldorp, C M, Rietschel, M, Nöthen, M M, Cichon, S, Gurling, H, Bass, N, McQuillin, A, Hamshere, M L, Craddock, N, Sklar, P & Smoller, J W 2010, ' Genome-wide association study of suicide attempts in mood disorder patients ', American Journal of Psychiatry, vol. 167, no. 12, pp. 1499-1507 . https://doi.org/10.1176/appi.ajp.2010.10040541
Family and twin studies suggest that liability for suicide attempts is heritable and distinct from mood disorder susceptibility. The authors therefore examined the association between common genomewide variation and lifetime suicide attempts.The auth
Bipolar Affective Puerperal Psychosis: Genome-Wide Significant Evidence for Linkage to Chromosome 16
Autor:
Ian Jones, Marian Hamshere, Jeanne-Marrie Nangle, Philip Bennett, Elaine Green, Jess Heron, Ricardo Segurado, David Lambert, Peter Holmans, Aiden Corvin, Mike Owen, Lisa Jones, Michael Gill, Nick Craddock
Publikováno v:
American Journal of Psychiatry. 164:1099-1104
Vulnerability to the triggering of bipolar episodes by childbirth aggregates in families and may define a genetically relevant subtype of bipolar disorder. The authors conducted a search by systematic whole genome linkage scan for loci influencing vu
Autor:
Jones, Lesley, Holmans, Peter A., Marian, Hamshere, Harold, Denise, Moskvina, Valentina, Ivanov, Dobril, Hardy, John, O'Donovan, Michael C., Owen, Michael, Williams, Julie
Publikováno v:
In Alzheimer's & Dementia: The Journal of the Alzheimer's Association July 2010 6(4) Supplement:S113-S113
Autor:
Michael C. O'Donovan, Nicholas Craddock, Nadine Norton, Hywel Williams, Timothy Peirce, Valentina Moskvina, Ivan Nikolov, Marian Hamshere, Liam Carroll, Lyudmila Georgieva, Sarah Dwyer, Peter Holmans, Jonathan L. Marchini, Chris C. A. Spencer, Bryan Howie, Hin-Tak Leung, Annette M. Hartmann, Hans-Jürgen Möller, Derek W. Morris, YongYong Shi
Publikováno v:
Nature Genetics; Sep2008, Vol. 40 Issue 9, p1053-1055, 3p, 2 Charts
Autor:
Evangelia Stergiakouli, Marian Hamshere, Peter Holmans, Kate Langley, Irina Zaharieva, Ziarah Hawi, Lindsey Kent, Michael Gill, Nigel Williams, Owen, Michael J., Donovan, Michael O., Anita Thapar, deCODE Genetics
Publikováno v:
University of Bristol-PURE
Stergiakouli, E, Hamshere, M, Holmans, P, Langley, K, Zaharieva, I, Hawi, Z, Kent, L, Gill, M, Williams, N, Owen, M J, O'Donovan, M, Thapar, A, deCODE Genetics & Steinhausen, H-C 2012, ' Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD ', American Journal of Psychiatry, vol. 169, no. 2, pp. 186-94 .
Stergiakouli, E, Hamshere, M, Holmans, P, Langley, K, Zaharieva, I, Hawi, Z, Kent, L, Gill, M, Williams, N, Owen, M J, O'Donovan, M, Thapar, A, deCODE Genetics & Steinhausen, H-C 2012, ' Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD ', American Journal of Psychiatry, vol. 169, no. 2, pp. 186-94 .
A major motivation for seeking disease-associated genetic variation is to identify novel risk processes. Although rare copy number variants (CNVs) appear to contribute to attention deficit hyperactivity disorder (ADHD), common risk variants (single-n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::77adcccf043c38f1046c189dc614f645
https://research-information.bris.ac.uk/en/publications/b68bf4c8-adc9-4013-a0d0-b38aad7975f3
https://research-information.bris.ac.uk/en/publications/b68bf4c8-adc9-4013-a0d0-b38aad7975f3